Determining targets for ceftriaxone resistance detection in Neisseria gonorrhoeae based on genotype-phenotype data: an observational study.

IF 20.4 1区 生物学 Q1 INFECTIOUS DISEASES
Sebastiaan J van Hal, Monica M Lahra, David M Whiley
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引用次数: 0

Abstract

Background: Increasing antimicrobial resistance to ceftriaxone in Neisseria gonorrhoeae presents a public health crisis. We aimed to identify a target associated with ceftriaxone resistance to support the development of rapid diagnostic tests.

Methods: In this observational study, we included N gonorrhoeae isolates with linked penA (NEIS1753) locus and ceftriaxone minimum inhibitory concentration (MIC) data. We compiled and collated isolate-level data from the international public databases PubMLST and Pathogenwatch, and publications up until March 1, 2025. We determined ceftriaxone resistance using the European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoint of an MIC of 0·250 mg/L or more and the WHO alert value of an MIC of 0·125 mg/L or more. We examined ceftriaxone resistance dynamics, with the sensitivity for susceptibility and resistance based on the constructed penA genotypes calculated.

Findings: We compiled 18 689 unique N gonorrhoeae isolates from 71 countries across all WHO regions, collected between 1971 and 2024. Using the EUCAST breakpoint, the overall ceftriaxone resistance rate was 2·4%, with evidence of increasing resistance over time. Analysis of MIC distributions revealed that two alleles, penA 60.001 and penA 237.001, both of the VMTAKGGP genotype, had MIC distributions predominantly above the resistance breakpoint. The VMTAKGGP genotype, defined by the A311V mutation, was associated with a sensitivity of 83·2% (95% CI 79·4-86·6) for detecting ceftriaxone resistance and 99·8% (99·7-99·9) for detecting sensitivity.

Interpretation: The A311V mutation is a key marker of ceftriaxone resistance. This target could inform the development of a molecular assay to detect ceftriaxone resistance.

Funding: Australian Research Council.

基于基因型-表型数据确定淋病奈瑟菌头孢曲松耐药检测靶点:一项观察性研究。
背景:淋病奈瑟菌对头孢曲松的耐药性日益增加,造成公共卫生危机。我们的目的是确定一个与头孢曲松耐药相关的靶点,以支持快速诊断测试的发展。方法:在这项观察性研究中,我们纳入了带有连接penA (NEIS1753)位点的N株淋病菌和头孢曲松最低抑制浓度(MIC)数据。我们从国际公共数据库PubMLST和Pathogenwatch以及截至2025年3月1日的出版物中汇编和整理了隔离级数据。我们使用欧洲抗微生物药物敏感性试验委员会(EUCAST)的MIC≥0.250 mg/L的断点和WHO的MIC≥0.125 mg/L的警戒值来确定头孢曲松耐药性。我们检测了头孢曲松的耐药动态,并计算了基于构建的penA基因型的敏感性和耐药性。研究结果:我们从1971年至2024年在世卫组织所有区域的71个国家收集了18689株独特的淋病奈恩菌分离株。使用EUCAST断点,头孢曲松总耐药率为2.4%,有证据表明耐药随时间增加。MIC分布分析显示,VMTAKGGP基因型的两个等位基因penA 60.001和penA 237.001的MIC分布主要在抗性断点以上。由A311V突变定义的VMTAKGGP基因型与头孢曲松耐药检测的敏感性相关,分别为83.2% (95% CI 79.4 ~ 86.6)和99.8%(99.7 ~ 99.9)。结论:A311V突变是头孢曲松耐药的关键标记。这个靶点可以为开发一种检测头孢曲松耐药性的分子测定方法提供信息。资助:澳大利亚研究委员会。
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来源期刊
Lancet Microbe
Lancet Microbe Multiple-
CiteScore
27.20
自引率
0.80%
发文量
278
审稿时长
6 weeks
期刊介绍: The Lancet Microbe is a gold open access journal committed to publishing content relevant to clinical microbiologists worldwide, with a focus on studies that advance clinical understanding, challenge the status quo, and advocate change in health policy.
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